ES2302038T3 - Agente activo como herbicida. - Google Patents

Agente activo como herbicida. Download PDF

Info

Publication number: ES2302038T3
Authority: ES; Spain
Prior art keywords: esters; liquid formulation; salts; plants; methyl
Prior art date: 2003-11-03
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Expired - Lifetime

Application number

ES04790700T

Other languages

English (en)

Spanish (es)

Inventor

Frank Ziemer

Gerhard Schnabel

Detlev Haase

Roland Deckwer

Christopher Rosinger

David Feist

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Bayer CropScience AG

Original Assignee

Bayer CropScience AG

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2003-11-03

Filing date

2004-10-21

Publication date

2008-07-01

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=34553322&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=ES2302038(T3) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

2003-11-03 Priority claimed from DE10351234A external-priority patent/DE10351234A1/de

2003-11-26 Priority claimed from DE10355846A external-priority patent/DE10355846A1/de

2004-10-21 Application filed by Bayer CropScience AG filed Critical Bayer CropScience AG

2008-07-01 Application granted granted Critical

2008-07-01 Publication of ES2302038T3 publication Critical patent/ES2302038T3/es

2024-10-21 Anticipated expiration legal-status Critical

Status Expired - Lifetime legal-status Critical Current

Links

239000004009 herbicide Substances 0.000 title claims description 43
239000013543 active substance Substances 0.000 title claims description 37
230000002363 herbicidal effect Effects 0.000 title claims description 18
-1 tifensulfuron Chemical compound 0.000 claims abstract description 70
150000002148 esters Chemical class 0.000 claims abstract description 55
239000000729 antidote Substances 0.000 claims abstract description 37
150000003839 salts Chemical class 0.000 claims abstract description 36
239000003921 oil Substances 0.000 claims abstract description 32
229940075522 antidotes Drugs 0.000 claims abstract description 31
229940100389 Sulfonylurea Drugs 0.000 claims abstract description 26
239000000725 suspension Substances 0.000 claims abstract description 17
239000002904 solvent Substances 0.000 claims abstract description 16
239000012141 concentrate Substances 0.000 claims abstract description 15
239000012669 liquid formulation Substances 0.000 claims abstract description 11
239000003960 organic solvent Substances 0.000 claims abstract description 9
ITGSCCPVERXFGN-UHFFFAOYSA-N isoxadifen Chemical compound C1C(C(=O)O)=NOC1(C=1C=CC=CC=1)C1=CC=CC=C1 ITGSCCPVERXFGN-UHFFFAOYSA-N 0.000 claims abstract description 7
ICJSJAJWTWPSBD-UHFFFAOYSA-N cloquintocet Chemical compound C1=CN=C2C(OCC(=O)O)=CC=C(Cl)C2=C1 ICJSJAJWTWPSBD-UHFFFAOYSA-N 0.000 claims abstract description 6
VJYIFXVZLXQVHO-UHFFFAOYSA-N chlorsulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)Cl)=N1 VJYIFXVZLXQVHO-UHFFFAOYSA-N 0.000 claims abstract description 5
UWHURBUBIHUHSU-UHFFFAOYSA-N 2-[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamoylsulfamoyl]benzoic acid Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 UWHURBUBIHUHSU-UHFFFAOYSA-N 0.000 claims abstract description 4
239000005626 Tribenuron Substances 0.000 claims abstract description 4
BQZXUHDXIARLEO-UHFFFAOYSA-N tribenuron Chemical compound COC1=NC(C)=NC(N(C)C(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 BQZXUHDXIARLEO-UHFFFAOYSA-N 0.000 claims abstract description 4
241000196324 Embryophyta Species 0.000 claims description 46
ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 claims description 21
239000000126 substance Substances 0.000 claims description 19
238000000034 method Methods 0.000 claims description 13
239000000654 additive Substances 0.000 claims description 12
230000000996 additive effect Effects 0.000 claims description 11
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238000002360 preparation method Methods 0.000 claims description 6
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230000009261 transgenic effect Effects 0.000 claims description 5
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235000021307 Triticum Nutrition 0.000 claims description 4
244000038559 crop plants Species 0.000 claims description 4
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235000011684 Sorghum saccharatum Nutrition 0.000 claims description 2
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244000098338 Triticum aestivum Species 0.000 claims 1
XEJNEDVTJPXRSM-UHFFFAOYSA-N 1-(2,4-dichlorophenyl)-5-methyl-4,5-dihydro-1H-pyrazole-3,5-dicarboxylic acid Chemical compound OC(=O)C1(C)CC(C(O)=O)=NN1C1=CC=C(Cl)C=C1Cl XEJNEDVTJPXRSM-UHFFFAOYSA-N 0.000 abstract description 2
239000000203 mixture Substances 0.000 description 42
235000014113 dietary fatty acids Nutrition 0.000 description 40
229930195729 fatty acid Natural products 0.000 description 40
239000000194 fatty acid Substances 0.000 description 40
235000019198 oils Nutrition 0.000 description 30
150000004665 fatty acids Chemical class 0.000 description 25
239000002253 acid Substances 0.000 description 22
238000009472 formulation Methods 0.000 description 20
YROXIXLRRCOBKF-UHFFFAOYSA-N sulfonylurea Chemical class OC(=N)N=S(=O)=O YROXIXLRRCOBKF-UHFFFAOYSA-N 0.000 description 17
239000002270 dispersing agent Substances 0.000 description 15
239000003795 chemical substances by application Substances 0.000 description 14
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150000004702 methyl esters Chemical class 0.000 description 13
229910052783 alkali metal Inorganic materials 0.000 description 11
125000000217 alkyl group Chemical group 0.000 description 11
125000004432 carbon atom Chemical group C* 0.000 description 11
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235000015112 vegetable and seed oil Nutrition 0.000 description 11
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229910052708 sodium Inorganic materials 0.000 description 10
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239000002562 thickening agent Substances 0.000 description 9
OVSKIKFHRZPJSS-UHFFFAOYSA-N 2,4-D Chemical compound OC(=O)COC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-UHFFFAOYSA-N 0.000 description 8
230000001804 emulsifying effect Effects 0.000 description 8
QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical class [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 7
150000001340 alkali metals Chemical class 0.000 description 7
125000005907 alkyl ester group Chemical group 0.000 description 7
150000001768 cations Chemical class 0.000 description 7
239000000463 material Substances 0.000 description 7
239000004094 surface-active agent Substances 0.000 description 7
238000005809 transesterification reaction Methods 0.000 description 7
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 6
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 6
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 6
150000007513 acids Chemical class 0.000 description 6
POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 6
125000004494 ethyl ester group Chemical group 0.000 description 6
IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 6
240000002791 Brassica napus Species 0.000 description 5
235000004977 Brassica sinapistrum Nutrition 0.000 description 5
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 5
150000001298 alcohols Chemical class 0.000 description 5
125000002947 alkylene group Chemical group 0.000 description 5
150000001408 amides Chemical class 0.000 description 5
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230000000694 effects Effects 0.000 description 5
238000005516 engineering process Methods 0.000 description 5
235000011187 glycerol Nutrition 0.000 description 5
238000000227 grinding Methods 0.000 description 5
229920000233 poly(alkylene oxides) Polymers 0.000 description 5
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UPMXNNIRAGDFEH-UHFFFAOYSA-N 3,5-dibromo-4-hydroxybenzonitrile Chemical compound OC1=C(Br)C=C(C#N)C=C1Br UPMXNNIRAGDFEH-UHFFFAOYSA-N 0.000 description 4
239000005489 Bromoxynil Substances 0.000 description 4
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 4
239000005977 Ethylene Substances 0.000 description 4
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
239000000443 aerosol Substances 0.000 description 4
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 4
150000001412 amines Chemical class 0.000 description 4
150000004945 aromatic hydrocarbons Chemical class 0.000 description 4
239000004359 castor oil Substances 0.000 description 4
235000019438 castor oil Nutrition 0.000 description 4
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
FOUWCSDKDDHKQP-UHFFFAOYSA-N flumioxazin Chemical compound FC1=CC=2OCC(=O)N(CC#C)C=2C=C1N(C1=O)C(=O)C2=C1CCCC2 FOUWCSDKDDHKQP-UHFFFAOYSA-N 0.000 description 4
ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 4
150000002314 glycerols Chemical class 0.000 description 4
239000002917 insecticide Substances 0.000 description 4
229910052751 metal Inorganic materials 0.000 description 4
239000002184 metal Substances 0.000 description 4
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
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WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 3
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QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 3
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YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
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ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 description 1
AKTQJCBOGPBERP-UHFFFAOYSA-N triflusulfuron Chemical compound FC(F)(F)COC1=NC(N(C)C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2C)C(O)=O)=N1 AKTQJCBOGPBERP-UHFFFAOYSA-N 0.000 description 1
IMEVJVISCHQJRM-UHFFFAOYSA-N triflusulfuron-methyl Chemical compound COC(=O)C1=CC=CC(C)=C1S(=O)(=O)NC(=O)NC1=NC(OCC(F)(F)F)=NC(N(C)C)=N1 IMEVJVISCHQJRM-UHFFFAOYSA-N 0.000 description 1
KVEQCVKVIFQSGC-UHFFFAOYSA-N tritosulfuron Chemical compound FC(F)(F)C1=NC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(F)(F)F)=N1 KVEQCVKVIFQSGC-UHFFFAOYSA-N 0.000 description 1
KJIOQYGWTQBHNH-UHFFFAOYSA-N undecanol Chemical compound CCCCCCCCCCCO KJIOQYGWTQBHNH-UHFFFAOYSA-N 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
235000020234 walnut Nutrition 0.000 description 1
238000001238 wet grinding Methods 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
239000010698 whale oil Substances 0.000 description 1
239000002023 wood Substances 0.000 description 1
239000008096 xylene Substances 0.000 description 1
150000003738 xylenes Chemical class 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/36—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< directly attached to at least one heterocyclic ring; Thio analogues thereof

Landscapes

Life Sciences & Earth Sciences (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

ES04790700T 2003-11-03 2004-10-21 Agente activo como herbicida. Expired - Lifetime ES2302038T3 (es)

Applications Claiming Priority (4)

Application Number	Priority Date	Filing Date	Title
DE10351234A DE10351234A1 (de)	2003-11-03	2003-11-03	Herbizid wirksames Mittel
DE10351234		2003-11-03
DE10355846A DE10355846A1 (de)	2003-11-26	2003-11-26	Herbizid wirksames Mittel
DE10355846		2003-11-26

Publications (1)

Publication Number	Publication Date
ES2302038T3 true ES2302038T3 (es)	2008-07-01

Family

ID=34553322

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
ES04790700T Expired - Lifetime ES2302038T3 (es)	2003-11-03	2004-10-21	Agente activo como herbicida.

Country Status (16)

Country	Link
US (2)	US7432226B2 (pl)
EP (1)	EP1681932B1 (pl)
AR (1)	AR046224A1 (pl)
AT (1)	ATE389327T1 (pl)
AU (1)	AU2004285269B2 (pl)
BR (1)	BRPI0416159A (pl)
CA (1)	CA2544415A1 (pl)
DE (1)	DE502004006612D1 (pl)
DK (1)	DK1681932T3 (pl)
EA (1)	EA012521B1 (pl)
ES (1)	ES2302038T3 (pl)
IL (1)	IL175359A0 (pl)
PL (1)	PL1681932T3 (pl)
TW (1)	TW200517058A (pl)
UA (1)	UA83698C2 (pl)
WO (1)	WO2005041654A2 (pl)

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PL3387904T3 (pl)	2014-12-22	2020-08-10	Mitsui Agriscience International S.A./N.V.	Ciekłe kompozycje chwastobójcze zawierające sulfonylomocznik
EP3236750B1 (en) *	2014-12-22	2019-10-30	Mitsui AgriScience International S.A./N.V.	Herbicidal oil dispersion
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JP2019535655A (ja)	2016-10-14	2019-12-12	ベーリンガーインゲルハイムアニマルヘルスユーエスエイインコーポレイテッド	殺虫性及び殺寄生虫性ビニルイソオキサゾリン化合物
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2004
- 2004-10-21 EP EP04790700A patent/EP1681932B1/de not_active Revoked
- 2004-10-21 CA CA002544415A patent/CA2544415A1/en not_active Abandoned
- 2004-10-21 ES ES04790700T patent/ES2302038T3/es not_active Expired - Lifetime
- 2004-10-21 PL PL04790700T patent/PL1681932T3/pl unknown
- 2004-10-21 DK DK04790700T patent/DK1681932T3/da active
- 2004-10-21 DE DE502004006612T patent/DE502004006612D1/de not_active Expired - Lifetime
- 2004-10-21 BR BRPI0416159-9A patent/BRPI0416159A/pt not_active IP Right Cessation
- 2004-10-21 WO PCT/EP2004/011893 patent/WO2005041654A2/de not_active Ceased
- 2004-10-21 AT AT04790700T patent/ATE389327T1/de not_active IP Right Cessation
- 2004-10-21 EA EA200600856A patent/EA012521B1/ru not_active IP Right Cessation
- 2004-10-21 UA UAA200606174A patent/UA83698C2/ru unknown
- 2004-10-21 AU AU2004285269A patent/AU2004285269B2/en not_active Ceased
- 2004-10-28 US US10/976,217 patent/US7432226B2/en not_active Expired - Lifetime
- 2004-11-01 AR ARP040104023A patent/AR046224A1/es not_active Application Discontinuation
- 2004-11-01 TW TW093133238A patent/TW200517058A/zh unknown
2006
- 2006-05-01 IL IL175359A patent/IL175359A0/en unknown
2008
- 2008-08-29 US US12/201,115 patent/US20090054236A1/en not_active Abandoned

Also Published As

Publication number	Publication date
CA2544415A1 (en)	2005-05-12
BRPI0416159A (pt)	2007-01-16
EP1681932B1 (de)	2008-03-19
US7432226B2 (en)	2008-10-07
TW200517058A (en)	2005-06-01
UA83698C2 (en)	2008-08-11
DE502004006612D1 (de)	2008-04-30
WO2005041654A3 (de)	2005-07-21
US20050113254A1 (en)	2005-05-26
AU2004285269A1 (en)	2005-05-12
AU2004285269B2 (en)	2010-07-01
IL175359A0 (en)	2006-09-05
WO2005041654A2 (de)	2005-05-12
EP1681932A2 (de)	2006-07-26
EA012521B1 (ru)	2009-10-30
PL1681932T3 (pl)	2008-08-29
EA200600856A1 (ru)	2006-10-27
AR046224A1 (es)	2005-11-30
US20090054236A1 (en)	2009-02-26
ATE389327T1 (de)	2008-04-15
DK1681932T3 (da)	2008-07-21

Publication	Publication Date	Title
AU2004285269B2 (en)	2010-07-01	Herbicidally active agent
ES2209561T5 (es)	2012-05-23	Combinaciones de herbicidas y antídotos
ES2229720T3 (es)	2005-04-16	Combinaciones de herbicidas y antidotos.
EP0790771B1 (de)	1999-01-20	Kombinationen aus phenylsulfonylharnstoff-herbiziden und safenern
JP5337798B2 (ja)	2013-11-06	グリセロール中の活性化合物懸濁剤
AU2009321765B2 (en)	2014-08-28	Dispersions comprising inhibitors of the hydroxyphenylpyruvate-dioxygenase
HRP20040246A2 (en)	2004-08-31	Herbicide and safening combinations
ES2532907T3 (es)	2015-04-01	Concentrado de suspensión en aceite
US6124240A (en)	2000-09-26	Combinations of sulfonylurea herbicides and safeners
ME00170B (me)	2010-06-10	Herbicidna suspenzija
BRPI0619385A2 (pt)	2011-10-04	formulações lìquidas contendo dialquilsulfossuccinatos e inibidores da hidroxifenilpiruvato-dioxigenase
DE10351234A1 (de)	2005-06-16	Herbizid wirksames Mittel
MXPA06004954A (en)	2006-10-17	Herbicidally active agent
DE10355846A1 (de)	2005-07-07	Herbizid wirksames Mittel
DE10351233A1 (de)	2005-06-02	Ölsuspensionskonzentrat
MX2008006918A (en)	2008-09-02	Liquid formulations containing dialkyl sulfosuccinate and hydroxyphenylpyruvate dioxygenase inhibitors